-
1
-
-
0037182703
-
Lucky draw in the gene raffle
-
Pollock, P. M. & Meltzer, P. S. Lucky draw in the gene raffle Nature 417, 906-907 (2002).
-
(2002)
Nature
, vol.417
, pp. 906-907
-
-
Pollock, P.M.1
Meltzer, P.S.2
-
2
-
-
18444374405
-
Mutations of the BRAF gene in human cancer
-
Davies, H. et al. Mutations of the BRAF gene in human cancer. Nature 417, 949-954 (2002).
-
(2002)
Nature
, vol.417
, pp. 949-954
-
-
Davies, H.1
-
3
-
-
0038697566
-
Raf proteins and cancer: B-Raf is identified as a mutational target
-
Mercer, K. E. & Pritchard, C. A. Raf proteins and cancer: B-Raf is identified as a mutational target. Biochim. Biophys. Acta 1653, 25-50 (2003).
-
(2003)
Biochim. Biophys. Acta
, vol.1653
, pp. 25-50
-
-
Mercer, K.E.1
Pritchard, C.A.2
-
4
-
-
0242361581
-
Transcriptional regulation by the MAP kinase signalling cascades
-
Yang, S. H., Sharrocks, A. D. & Whitmarsh, A. J. Transcriptional regulation by the MAP kinase signalling cascades. Gene 320, 3-21 (2003).
-
(2003)
Gene
, vol.320
, pp. 3-21
-
-
Yang, S.H.1
Sharrocks, A.D.2
Whitmarsh, A.J.3
-
5
-
-
0037228055
-
High frequency of BRAF mutations in nevi
-
Pollock P. M. et al. High frequency of BRAF mutations in nevi. Nature Genet. 33, 595-602 (2003).
-
(2003)
Nature Genet.
, vol.33
, pp. 595-602
-
-
Pollock, P.M.1
-
6
-
-
12144289677
-
Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF
-
Wan, P. T. C. et al. Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF. Cell 116, 855-867 (2004).
-
(2004)
Cell
, vol.116
, pp. 855-867
-
-
Wan, P.T.C.1
-
7
-
-
0027359443
-
Identification of mutations in the coding sequence of the proto-oncogene c-kit in a human mast cell leukaemia cell line causing ligand-independent activation of c-kit product
-
Furitsu, T. et al. Identification of mutations in the coding sequence of the proto-oncogene c-kit in a human mast cell leukaemia cell line causing ligand-independent activation of c-kit product. J. Clin. Invest. 92, 1736-1744 (1993).
-
(1993)
J. Clin. Invest.
, vol.92
, pp. 1736-1744
-
-
Furitsu, T.1
-
8
-
-
0028790864
-
Selection of activating mutations of c-fms in FDC-P1 cells
-
Glover, H. R., Baker, D. A., Celetti, A. & Dibb, N. J. Selection of activating mutations of c-fms in FDC-P1 cells. Oncogene 11, 1347-1356 (1995).
-
(1995)
Oncogene
, vol.11
, pp. 1347-1356
-
-
Glover, H.R.1
Baker, D.A.2
Celetti, A.3
Dibb, N.J.4
-
9
-
-
32344441627
-
Proteomic approaches to the analysis of early events in colony-stimulating factor-1 signal transduction
-
Yeung, Y.-G. & Stanley, E. R. Proteomic approaches to the analysis of early events in colony-stimulating factor-1 signal transduction. Mol. Cell. Proteomics 2, 1143-1155.
-
Mol. Cell. Proteomics
, vol.2
, pp. 1143-1155
-
-
Yeung, Y.-G.1
Stanley, E.R.2
-
10
-
-
0028252924
-
Steel factor and c-kit protooncogene: Genetic lessons in signal transduction
-
Lev, S., Blechman, J. M., Givol, D. & Yarden, Y. Steel factor and c-kit protooncogene: genetic lessons in signal transduction. Crit. Rev. Oncog. 5, 141-168 (1994).
-
(1994)
Crit. Rev. Oncog.
, vol.5
, pp. 141-168
-
-
Lev, S.1
Blechman, J.M.2
Givol, D.3
Yarden, Y.4
-
11
-
-
0032875460
-
Mechanism of action and in vivo role of platelet-derived growth factor
-
Heldin, C. H. & Westermark, B. Mechanism of action and in vivo role of platelet-derived growth factor. Physiol. Rev. 79, 1283-1316 (1999).
-
(1999)
Physiol. Rev.
, vol.79
, pp. 1283-1316
-
-
Heldin, C.H.1
Westermark, B.2
-
12
-
-
0141465061
-
The role of FLT3 in haematopoietic malignancies
-
Stirewalt, D. L. & Radich, J. P. The role of FLT3 in haematopoietic malignancies. Nature Rev. Cancer 3, 650-665 (2003).
-
(2003)
Nature Rev. Cancer
, vol.3
, pp. 650-665
-
-
Stirewalt, D.L.1
Radich, J.P.2
-
13
-
-
0025343230
-
Signal transduction by receptors with tyrosine kinase activity
-
Ullrich, A. & Schlessinger, J. Signal transduction by receptors with tyrosine kinase activity. Cell 61, 203-212 (1990).
-
(1990)
Cell
, vol.61
, pp. 203-212
-
-
Ullrich, A.1
Schlessinger, J.2
-
14
-
-
0031015002
-
CSF-1 and its receptor in breast carcinomas and neoplasms of the female reproductive tract
-
Kacinski, B. M. CSF-1 and its receptor in breast carcinomas and neoplasms of the female reproductive tract. Mol. Reprod. Dev. 46, 71-74 (1997).
-
(1997)
Mol. Reprod. Dev.
, vol.46
, pp. 71-74
-
-
Kacinski, B.M.1
-
15
-
-
0028856070
-
Identification of a point mutation in the catalytic domain of the proto-oncogene c-kit in peripheral blood mononuclear cells of patients who have mastocytosis with an associated hematologic disorder
-
Nagata, H. et al. Identification of a point mutation in the catalytic domain of the proto-oncogene c-kit in peripheral blood mononuclear cells of patients who have mastocytosis with an associated hematologic disorder. Proc. Natl Acad. Sci USA 92, 10560-10564 (1995).
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 10560-10564
-
-
Nagata, H.1
-
16
-
-
0036124762
-
Class III receptor tyrosine kinases: Role in leukaemogenesis
-
Reilly J. T. Class III receptor tyrosine kinases: role in leukaemogenesis. Br. J. Haematol. 116, 744-757 (2002).
-
(2002)
Br. J. Haematol.
, vol.116
, pp. 744-757
-
-
Reilly, J.T.1
-
17
-
-
15644363454
-
Gain of function mutations of c-kit in human gastrointestinal stromal tumours
-
Hirota, S. et al. Gain of function mutations of c-kit in human gastrointestinal stromal tumours. Science 279, 577-580 (1998).
-
(1998)
Science
, vol.279
, pp. 577-580
-
-
Hirota, S.1
-
18
-
-
1542784354
-
KIT mutations are common in testicular seminomas
-
Kemmer, K. et al. KIT mutations are common in testicular seminomas. Am. J. Pathol. 164, 305-313 (2004).
-
(2004)
Am. J. Pathol.
, vol.164
, pp. 305-313
-
-
Kemmer, K.1
-
19
-
-
0041971080
-
Gain-of-function mutations of platelet-derived growth factor receptor α gene in gastrointestinal stromal tumours
-
Hirota, S. et al. Gain-of-function mutations of platelet-derived growth factor receptor α gene in gastrointestinal stromal tumours. Gastroenterology 125, 660-667 (2003).
-
(2003)
Gastroenterology
, vol.125
, pp. 660-667
-
-
Hirota, S.1
-
20
-
-
0242670019
-
PDGFRA activating mutations in gastrointestinal stromal tumours
-
Heinrich, M. C. et al. PDGFRA activating mutations in gastrointestinal stromal tumours. Science 299, 708-710 (2003).
-
(2003)
Science
, vol.299
, pp. 708-710
-
-
Heinrich, M.C.1
-
21
-
-
0028959163
-
Constitutively activating mutations of c-kit receptor tyrosine kinase confer factor-independent growth and tumorigenicity of factor-dependent hematopoietic cell lines
-
Kitayama, H. et al. Constitutively activating mutations of c-kit receptor tyrosine kinase confer factor-independent growth and tumorigenicity of factor-dependent hematopoietic cell lines. Blood 85, 790-798 (1995).
-
(1995)
Blood
, vol.85
, pp. 790-798
-
-
Kitayama, H.1
-
22
-
-
0029993727
-
Active and inactive protein kinases: Structural basis for regulation
-
Johnson, L. N., Noble, M. E. M. & Owen, D. J. Active and inactive protein kinases: structural basis for regulation. Cell 85, 149-158 (1996).
-
(1996)
Cell
, vol.85
, pp. 149-158
-
-
Johnson, L.N.1
Noble, M.E.M.2
Owen, D.J.3
-
23
-
-
0037032835
-
The protein kinase complement of the human genome
-
Manning, G., Whyte, D. B., Martinez, R., Hunter, T. & Sudarsanam, S. The protein kinase complement of the human genome. Science 298, 1912-1934 (2002).
-
(2002)
Science
, vol.298
, pp. 1912-1934
-
-
Manning, G.1
Whyte, D.B.2
Martinez, R.3
Hunter, T.4
Sudarsanam, S.5
-
24
-
-
0037013143
-
The conformational plasticity of protein kinases
-
Huse, M. & Kuriyan, J. The conformational plasticity of protein kinases. Cell 109, 275-282 (2002).
-
(2002)
Cell
, vol.109
, pp. 275-282
-
-
Huse, M.1
Kuriyan, J.2
-
25
-
-
0026342401
-
Crystal structure of the catalytic subunit of cyclic adenosine monophosphate-dependent protein kinase
-
Knighton, D. R., et al. Crystal structure of the catalytic subunit of cyclic adenosine monophosphate-dependent protein kinase. Science 253, 407-414 (1991).
-
(1991)
Science
, vol.253
, pp. 407-414
-
-
Knighton, D.R.1
-
26
-
-
0028582185
-
Crystal structure of the tyrosine kinase domain of the human insulin receptor
-
Hubbard, S. R., Ellis, L. & Hendrickson, W. A. Crystal structure of the tyrosine kinase domain of the human insulin receptor. Nature 372, 748-754 (1994).
-
(1994)
Nature
, vol.372
, pp. 748-754
-
-
Hubbard, S.R.1
Ellis, L.2
Hendrickson, W.A.3
-
27
-
-
0030766163
-
Crystal structure of the activated insulin receptor tyrosine kinase in complex with peptide substrate and ATP analog
-
Hubbard, S. R. Crystal structure of the activated insulin receptor tyrosine kinase in complex with peptide substrate and ATP analog. EMBO J. 16, 5573-5581 (1997).
-
(1997)
EMBO J.
, vol.16
, pp. 5573-5581
-
-
Hubbard, S.R.1
-
28
-
-
0034793734
-
Crystal structure of bisphosphorylated IGF-1 receptor kinase: Insight into domain movements upon kinase activation
-
Pautsch, A. et al. Crystal structure of bisphosphorylated IGF-1 receptor kinase: insight into domain movements upon kinase activation. Structure 9, 955-965 (2001).
-
(2001)
Structure
, vol.9
, pp. 955-965
-
-
Pautsch, A.1
-
29
-
-
0037064032
-
Crystal structure of the Apo, unactivated insulin-like growth factor-1 receptor kinase
-
Munshi, S. et al. Crystal structure of the Apo, unactivated insulin-like growth factor-1 receptor kinase. J. Biol. Chem. 277, 38797-38802 (2001).
-
(2001)
J. Biol. Chem.
, vol.277
, pp. 38797-38802
-
-
Munshi, S.1
-
30
-
-
0042357240
-
Structure of a c-Kit product complex reveals the basis for kinase transactivation
-
Mol, C. D. et al. Structure of a c-Kit product complex reveals the basis for kinase transactivation. J. Biol. Chem. 278, 31461-31464 (2003).
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 31461-31464
-
-
Mol, C.D.1
-
31
-
-
2942542387
-
Structural basis for the autoinhibition and STI-571 inhibition of c-Kit tyrosine kinase
-
Mol, C. D. et al. Structural basis for the autoinhibition and STI-571 inhibition of c-Kit tyrosine kinase. J. Biol. Chem. 279, 31655-31663.
-
J. Biol. Chem.
, vol.279
, pp. 31655-31663
-
-
Mol, C.D.1
-
32
-
-
16144364951
-
Structural basis for activation of human lymphocyte kinase Lck upon tyrosine phosphorylation
-
Yamaguchi, H. & Hendrickson W. A. Structural basis for activation of human lymphocyte kinase Lck upon tyrosine phosphorylation. Nature 348, 484-489 (1996).
-
(1996)
Nature
, vol.348
, pp. 484-489
-
-
Yamaguchi, H.1
Hendrickson, W.A.2
-
33
-
-
0033063429
-
Crystal structure of Hck in complex with a Src family-selective tyrosine kinase inhibitor
-
Schindler, T. et al. Crystal structure of Hck in complex with a Src family-selective tyrosine kinase inhibitor. Mol. Cell 3, 639-648 (1999).
-
(1999)
Mol. Cell
, vol.3
, pp. 639-648
-
-
Schindler, T.1
-
34
-
-
18744373865
-
Crystal structure of an activated Akt/protein kinase B ternary complex with GSK3-peptide and AMP-PNP
-
Yang, J. et al. Crystal structure of an activated Akt/protein kinase B ternary complex with GSK3-peptide and AMP-PNP. Nature Struct. Biol. 9, 940-944 (2002).
-
(2002)
Nature Struct. Biol.
, vol.9
, pp. 940-944
-
-
Yang, J.1
-
35
-
-
0036295728
-
Molecular mechanism for the regulation of protein kinase B/Akt by hydrophobic motif phosphorylation
-
Yang, J. et al. Molecular mechanism for the regulation of protein kinase B/Akt by hydrophobic motif phosphorylation. Mol. Cell 9, 1227-1240 (2002).
-
(2002)
Mol. Cell
, vol.9
, pp. 1227-1240
-
-
Yang, J.1
-
36
-
-
0030911867
-
The structure of mitogen-activated protein kinase p38 at 2.1-A resolution
-
Wang, Z., Harkins, P. C., Ulevitch, R. J., Cobb, M. H. & Goldsmith, E. J. The structure of mitogen-activated protein kinase p38 at 2.1-A resolution. Proc. Natl Acad. Sci. USA 94, 2327-2332 (1997).
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 2327-2332
-
-
Wang, Z.1
Harkins, P.C.2
Ulevitch, R.J.3
Cobb, M.H.4
Goldsmith, E.J.5
-
37
-
-
0033567706
-
The structure of phosphorylated p38γ is monomeric and reveals a conserved activation-loop conformation
-
Bellon, S., Fitzgibbon, M. J., Fox, T. & Hsiao, H. M. & Wilson K. P. The structure of phosphorylated p38γ is monomeric and reveals a conserved activation-loop conformation. Structure Fold Des. 7, 1057-1065 (1999).
-
(1999)
Structure Fold Des.
, vol.7
, pp. 1057-1065
-
-
Bellon, S.1
Fitzgibbon, M.J.2
Fox, T.3
Hsiao, H.M.4
Wilson, K.P.5
-
38
-
-
0030866897
-
Activation mechanism of the MAP Kinase ERK2 by dual phosphorylation
-
Canagarajah, B. J., Khokhlatchev, A., Cobb, M. H. & Goldsmith, E. J. Activation mechanism of the MAP Kinase ERK2 by dual phosphorylation. Cell 90, 859-869 (1997).
-
(1997)
Cell
, vol.90
, pp. 859-869
-
-
Canagarajah, B.J.1
Khokhlatchev, A.2
Cobb, M.H.3
Goldsmith, E.J.4
-
39
-
-
0035990907
-
Structural aspects of protein kinase control - Role of conformational flexibility
-
Engh, R. A. & Bossenmeyer, D. Structural aspects of protein kinase control - role of conformational flexibility. Pharmacol. Ther. 93, 99-111 (2002).
-
(2002)
Pharmacol. Ther.
, vol.93
, pp. 99-111
-
-
Engh, R.A.1
Bossenmeyer, D.2
-
40
-
-
0027182223
-
Crystal structure of cyclin-dependent kinase 2
-
De Bondt, H. et al. Crystal structure of cyclin-dependent kinase 2. Nature 363, 595-602 (1993).
-
(1993)
Nature
, vol.363
, pp. 595-602
-
-
De Bondt, H.1
-
41
-
-
0029029617
-
Mechanism of CDK activation revealed by the structure of a cyclin-A CDK2 complex
-
Jeffrey, P. D. et al. Mechanism of CDK activation revealed by the structure of a cyclin-A CDK2 complex. Nature 376, 313-320 (1995).
-
(1995)
Nature
, vol.376
, pp. 313-320
-
-
Jeffrey, P.D.1
-
42
-
-
0347520938
-
Specificity determinants of recruitment peptides bound to phospho-CDK2/cyclin A
-
Lowe, E. D. et al. Specificity determinants of recruitment peptides bound to phospho-CDK2/cyclin A. Biochemistry 41, 15625-15634 (2002).
-
(2002)
Biochemistry
, vol.41
, pp. 15625-15634
-
-
Lowe, E.D.1
-
43
-
-
0035754080
-
To cycle or not to cycle: A critical decision in cancer
-
Malumbres, M. & Barbacid, M. To cycle or not to cycle: a critical decision in cancer. Nature Rev. Cancer 1, 222-231 (2001).
-
(2001)
Nature Rev. Cancer
, vol.1
, pp. 222-231
-
-
Malumbres, M.1
Barbacid, M.2
-
44
-
-
0029767016
-
Structural basis of cyclin-dependent kinase activation by phosphorylation
-
Russo, A. A., Jeffrey, P. D. & Pavletich, N. P. Structural basis of cyclin-dependent kinase activation by phosphorylation. Nature Struct. Biol. 3, 696-700 (1996).
-
(1996)
Nature Struct. Biol.
, vol.3
, pp. 696-700
-
-
Russo, A.A.1
Jeffrey, P.D.2
Pavletich, N.P.3
-
45
-
-
0141599428
-
Structure of the epidermal growth factor receptor kinase domain alone and in complex with a 4-anilinoquinazoline inhibitor
-
Stamos, J., Sliwkowski, M. X. & Eigenbrot, C. Structure of the epidermal growth factor receptor kinase domain alone and in complex with a 4-anilinoquinazoline inhibitor. J. Biol. Chem. 277, 46265-46272 (2002).
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 46265-46272
-
-
Stamos, J.1
Sliwkowski, M.X.2
Eigenbrot, C.3
-
46
-
-
0034665713
-
Structural mechanism for STI-571 inhibition of abelson tyrosine kinase
-
Schindler, T., Bornmann, W., Pellicena, P., Miller, W. T., Clarkson, B. & Kuriyan, J. Structural mechanism for STI-571 inhibition of abelson tyrosine kinase. Science 289, 1938-1942 (2000).
-
(2000)
Science
, vol.289
, pp. 1938-1942
-
-
Schindler, T.1
Bornmann, W.2
Pellicena, P.3
Miller, W.T.4
Clarkson, B.5
Kuriyan, J.6
-
47
-
-
3042716081
-
A single amino acid exchange inverts susceptibility of related receptor tyrosine kinases for the ATP site inhibitor STI-571
-
Bohmer, F. D. et al. A single amino acid exchange inverts susceptibility of related receptor tyrosine kinases for the ATP site inhibitor STI-571. J. Biol. Chem. 278, 5148-5155 (2003).
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 5148-5155
-
-
Bohmer, F.D.1
-
48
-
-
0034675919
-
Activation of B-Raf kinase requires phosphorylation of the conserved residues Thr598 and Ser601
-
Zhang, B. H. & Guan K. L. Activation of B-Raf kinase requires phosphorylation of the conserved residues Thr598 and Ser601. EMBO J. 19, 5429-5439 (2000).
-
(2000)
EMBO J.
, vol.19
, pp. 5429-5439
-
-
Zhang, B.H.1
Guan, K.L.2
-
49
-
-
0037405026
-
Autoinhibition of the Kit receptor tyrosine kinase by the cytosolic juxtamembrane region
-
Chan, P. M., Ilangumaran, S., La Rose, J., Chakrabartty, A. & Rottapel, R. Autoinhibition of the Kit receptor tyrosine kinase by the cytosolic juxtamembrane region. Mol. Cell. Biol. 23, 3067-3078 (2003).
-
(2003)
Mol. Cell. Biol.
, vol.23
, pp. 3067-3078
-
-
Chan, P.M.1
Ilangumaran, S.2
La Rose, J.3
Chakrabartty, A.4
Rottapel, R.5
-
50
-
-
0035929146
-
Structural basis for autoinhibition of the EphB2 receptor tyrosine kinase by the unphosphorylated juxtamembrane region
-
Wybenga-Groot, L. et al Structural basis for autoinhibition of the EphB2 receptor tyrosine kinase by the unphosphorylated juxtamembrane region. Cell 106, 745-757 (2001).
-
(2001)
Cell
, vol.106
, pp. 745-757
-
-
Wybenga-Groot, L.1
-
51
-
-
0038168241
-
Structural and biochemical evidence for an autoinhibitory role for tyrosine 984 in the juxtamembrane region of the insulin receptor
-
Li, S., Covino, N. D., Stein, E. G., Till, J. H. & Hubbard, S. R. Structural and biochemical evidence for an autoinhibitory role for tyrosine 984 in the juxtamembrane region of the insulin receptor. J. Biol. Chem. 278, 26007-26014 (2003).
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 26007-26014
-
-
Li, S.1
Covino, N.D.2
Stein, E.G.3
Till, J.H.4
Hubbard, S.R.5
-
52
-
-
0033524943
-
Crystal structure of the cytoplasmic domain of the type I TGFβ receptor in complex with FKBP12
-
Huse, M., Chen, Y.-G., Massague, J. & Kuriyan, J. Crystal structure of the cytoplasmic domain of the type I TGFβ receptor in complex with FKBP12. Cell 96, 425-436 (1999).
-
(1999)
Cell
, vol.96
, pp. 425-436
-
-
Huse, M.1
Chen, Y.-G.2
Massague, J.3
Kuriyan, J.4
-
53
-
-
0842310394
-
The structural basis for autoinhibition of FLT3 by the juxtamembrane domain
-
Griffith, J. et al. The structural basis for autoinhibition of FLT3 by the juxtamembrane domain. Mol. Cell 13, 169-178 (2004).
-
(2004)
Mol. Cell
, vol.13
, pp. 169-178
-
-
Griffith, J.1
-
54
-
-
0033587101
-
Cell specific transformation by c-fms activating loop mutations is attributable to constitutive receptor degradation
-
Morley, G. M., Uden, M., Gullick, W. J. & Dibb, N. J. Cell specific transformation by c-fms activating loop mutations is attributable to constitutive receptor degradation. Oncogene 18, 3076-3084 (1999).
-
(1999)
Oncogene
, vol.18
, pp. 3076-3084
-
-
Morley, G.M.1
Uden, M.2
Gullick, W.J.3
Dibb, N.J.4
-
55
-
-
0036493872
-
The c-KIT mutation causing human mastocytosis is resistant to STI571 and other kinase inhibitors; kinases with enzymatic site mutations show different inhibitor sensitivity profiles than wild-type kinases and those with regulatory-type mutations
-
Ma, Y. et al. The c-KIT mutation causing human mastocytosis is resistant to STI571 and other kinase inhibitors; kinases with enzymatic site mutations show different inhibitor sensitivity profiles than wild-type kinases and those with regulatory-type mutations. Blood 99, 1741-1744 (2002).
-
(2002)
Blood
, vol.99
, pp. 1741-1744
-
-
Ma, Y.1
-
56
-
-
0034993741
-
Classes of c-KIT activating mutations: Proposed mechanisms of action and implications for disease classification and therapy
-
Longley, B. J., Reguera, M. J. & Ma, Y. Classes of c-KIT activating mutations: proposed mechanisms of action and implications for disease classification and therapy. Leuk. Res. 25, 571-576 (2001).
-
(2001)
Leuk. Res.
, vol.25
, pp. 571-576
-
-
Longley, B.J.1
Reguera, M.J.2
Ma, Y.3
-
57
-
-
0344987886
-
Effect of tyrosine kinase inhibitor STI571 on the kinase activity of wild-type and various mutated c-kit receptors found in mast cell neoplasm
-
Zermati, Y. et al. Effect of tyrosine kinase inhibitor STI571 on the kinase activity of wild-type and various mutated c-kit receptors found in mast cell neoplasm. Oncogene 22, 660-664 (2003).
-
(2003)
Oncogene
, vol.22
, pp. 660-664
-
-
Zermati, Y.1
-
58
-
-
0030023799
-
Role of aspartic acid 814 in the function and expression of c-kit receptor tyrosine kinase
-
Moriyama, Y. et al. Role of aspartic acid 814 in the function and expression of c-kit receptor tyrosine kinase. J. Biol. Chem. 271, 3347-3350 (1996).
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 3347-3350
-
-
Moriyama, Y.1
-
59
-
-
0030031766
-
Inhibition of the Abl protein-tyrosine kinase in vitro and in vivo by a 2-phenylaminopyrimidine derivative
-
Buchdunger, E. et al. Inhibition of the Abl protein-tyrosine kinase in vitro and in vivo by a 2-phenylaminopyrimidine derivative. Cancer Res. 56, 100-104 (1996).
-
(1996)
Cancer Res.
, vol.56
, pp. 100-104
-
-
Buchdunger, E.1
-
60
-
-
0035810147
-
Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukaemia
-
Druker, B. J. et al. Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukaemia. N. Engl. J. Med. 344, 1031-1037 (2001).
-
(2001)
N. Engl. J. Med.
, vol.344
, pp. 1031-1037
-
-
Druker, B.J.1
-
61
-
-
0036846345
-
Management of malignant gastrointestinal stromal tumours
-
Joensuu, H. et al. Management of malignant gastrointestinal stromal tumours. Lancet Oncol. 3, 655-664 (2002).
-
(2002)
Lancet Oncol.
, vol.3
, pp. 655-664
-
-
Joensuu, H.1
-
62
-
-
0036560577
-
Oncogenic tyrosine kinases and the DNA-damage response
-
Skorski, T. Oncogenic tyrosine kinases and the DNA-damage response. Nature Rev. Cancer 2, 351-360 (2002).
-
(2002)
Nature Rev. Cancer
, vol.2
, pp. 351-360
-
-
Skorski, T.1
-
63
-
-
0033816156
-
Abl protein-tyrosine kinase inhibitor STI571 inhibits in vitro signal transduction mediated by c-Kit and platelet-derived growth factor receptors
-
Buchdunger, E. et al. Abl protein-tyrosine kinase inhibitor STI571 inhibits in vitro signal transduction mediated by c-Kit and platelet-derived growth factor receptors. J. Pharmacol. Exp. Ther. 295, 139-145 (2000).
-
(2000)
J. Pharmacol. Exp. Ther.
, vol.295
, pp. 139-145
-
-
Buchdunger, E.1
-
64
-
-
0037103624
-
Response to imatinib mesylate in patients with chronic myeloproliferative diseases with rearrangements of the platelet-derived growth factor receptor β
-
Apperley, J. F. et al. Response to imatinib mesylate in patients with chronic myeloproliferative diseases with rearrangements of the platelet-derived growth factor receptor β. N. Engl. J. Med. 347, 481-487 (2002).
-
(2002)
N. Engl. J. Med.
, vol.347
, pp. 481-487
-
-
Apperley, J.F.1
-
65
-
-
0141486251
-
PDGF receptors as cancer drug targets
-
Pietras, K., Sjoblom, T., Rubin, K., Heldin, C.-H. & Ostman, A. PDGF receptors as cancer drug targets. Cancer Cell 3, 439-443 (2003).
-
(2003)
Cancer Cell
, vol.3
, pp. 439-443
-
-
Pietras, K.1
Sjoblom, T.2
Rubin, K.3
Heldin, C.-H.4
Ostman, A.5
-
66
-
-
0001686739
-
Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukaemia
-
Shah, N. P. et al. Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukaemia. Cancer Cell 2, 117-125 (2002).
-
(2002)
Cancer Cell
, vol.2
, pp. 117-125
-
-
Shah, N.P.1
-
67
-
-
0037315281
-
Molecular mechanisms of resistance to imatinib in Philadelphia- chromosome-positive leukaemias
-
Gambacorti-Passerini, C. B. et al. Molecular mechanisms of resistance to imatinib in Philadelphia-chromosome-positive leukaemias. Lancet Oncol. 4, 75-85 (2003).
-
(2003)
Lancet Oncol.
, vol.4
, pp. 75-85
-
-
Gambacorti-Passerini, C.B.1
-
68
-
-
0037459341
-
Variation on an Src-like theme
-
Harrison, S. C. Variation on an Src-like theme. Cell 112, 737-740 (2003).
-
(2003)
Cell
, vol.112
, pp. 737-740
-
-
Harrison, S.C.1
-
69
-
-
0037459344
-
Mechanisms of autoinhibition and STI-571/Imatinib resistance revealed by mutagenesis of BCR-ABL
-
Azam, M., Latek, R. R. & Daley, G. Q. Mechanisms of autoinhibition and STI-571/Imatinib resistance revealed by mutagenesis of BCR-ABL. Cell 112, 831-843 (2003).
-
(2003)
Cell
, vol.112
, pp. 831-843
-
-
Azam, M.1
Latek, R.R.2
Daley, G.Q.3
-
70
-
-
0344395603
-
Bypassing a kinase activity with an ATP-competitive drug
-
Papa, F. R., Zhang, C., Shokat, K. & Walter P. Bypassing a kinase activity with an ATP-competitive drug. Science 302, 1533-1537 (2003).
-
(2003)
Science
, vol.302
, pp. 1533-1537
-
-
Papa, F.R.1
Zhang, C.2
Shokat, K.3
Walter, P.4
-
71
-
-
0036909260
-
Protein tyrosine kinases: Autoregulation and small-molecule inhibition
-
Hubbard, S. R. Protein tyrosine kinases: autoregulation and small-molecule inhibition. Curr. Opin. Struct. Biol. 12, 735-741 (2002).
-
(2002)
Curr. Opin. Struct. Biol.
, vol.12
, pp. 735-741
-
-
Hubbard, S.R.1
-
72
-
-
0344626926
-
Structural basis for the autoinhibition of c-Abl tyrosine kinase
-
Nagar, B. et al. Structural basis for the autoinhibition of c-Abl tyrosine kinase. Cell 112, 859-871 (2003).
-
(2003)
Cell
, vol.112
, pp. 859-871
-
-
Nagar, B.1
-
73
-
-
0036595322
-
Finding the next Gleevec: FLT3 targeted kinase inhibitor therapy for acute myeloid leukaemia
-
Sawyers, C. L. Finding the next Gleevec: FLT3 targeted kinase inhibitor therapy for acute myeloid leukaemia. Cancer Cell 1, 413-415 (2002).
-
(2002)
Cancer Cell
, vol.1
, pp. 413-415
-
-
Sawyers, C.L.1
-
74
-
-
0035911221
-
Colony stimulating factor 1 promotes progression of mammary tumours to malignancy
-
Lin, E. Y., Nguyen, A. V., Russell, R. G. & Pollard, J. W. Colony stimulating factor 1 promotes progression of mammary tumours to malignancy. J. Exp Med. 193, 727-740 (2001).
-
(2001)
J. Exp. Med.
, vol.193
, pp. 727-740
-
-
Lin, E.Y.1
Nguyen, A.V.2
Russell, R.G.3
Pollard, J.W.4
-
75
-
-
9144274970
-
SU11248 inhibits tumor growth and CSF-1R dependent osteolysis in an experimental breast cancer bone metastasis model
-
Murray, L. J. et al. SU11248 inhibits tumor growth and CSF-1R dependent osteolysis in an experimental breast cancer bone metastasis model. Clin. Exp. Mestastasis 20, 757-766 (2003).
-
(2003)
Clin. Exp. Mestastasis
, vol.20
, pp. 757-766
-
-
Murray, L.J.1
-
76
-
-
0038670241
-
Mutational analysis of the tyrosine kinome in colorectal cancers
-
Bardelli, A. et al. Mutational analysis of the tyrosine kinome in colorectal cancers. Science 300, 949 (2003).
-
(2003)
Science
, vol.300
, pp. 949
-
-
Bardelli, A.1
-
77
-
-
0034213931
-
RTK mutations and human syndromes: When good receptors turn bad
-
Robertson, S. C., Tynan, J. A. & Donoghue, D. J. RTK mutations and human syndromes: when good receptors turn bad. Trends Genet. 16, 265-271 (2000).
-
(2000)
Trends Genet.
, vol.16
, pp. 265-271
-
-
Robertson, S.C.1
Tynan, J.A.2
Donoghue, D.J.3
-
78
-
-
2342471392
-
Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to Gefitinib
-
Lynch, T. J. et al. Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to Gefitinib. N. Engl. J. Med. 350, 2129-2139 (2004)
-
(2004)
N. Engl. J. Med.
, vol.350
, pp. 2129-2139
-
-
Lynch, T.J.1
-
79
-
-
2342624080
-
EGFR mutations in lung cancer: Correlation with clinical response to gefitinib therapy
-
Paez, J. G. EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy. Science 304, 1497-1500 (2004).
-
(2004)
Science
, vol.304
, pp. 1497-1500
-
-
Paez, J.G.1
-
80
-
-
0141817701
-
The discovery of the α-helix and β-sheet, the principal structural features of proteins
-
Eisenberg, D. The discovery of the α-helix and β-sheet, the principal structural features of proteins. Proc. Natl Acad. Sci. USA 100, 11207-11210 (2003).
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 11207-11210
-
-
Eisenberg, D.1
-
81
-
-
0033532190
-
Inhibition of spontaneous receptor phosphorylation by residues in a putative α-helix in the KIT intracellular region
-
Ma, Y. et al. Inhibition of spontaneous receptor phosphorylation by residues in a putative α-helix in the KIT intracellular region. J. Biol. Chem. 274, 13399-13402 (1999).
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 13399-13402
-
-
Ma, Y.1
-
82
-
-
10744225271
-
Association of KIT exon 9 mutations with nongastric primary site and aggressive behaviour: KIT analysis and clinical correlates of 120 gastrointestinal stromal tumours
-
Antonescu, C. R. et al. Association of KIT exon 9 mutations with nongastric primary site and aggressive behaviour: KIT analysis and clinical correlates of 120 gastrointestinal stromal tumours. Clin. Cancer Res. 9, 3329-3337 (2003).
-
(2003)
Clin. Cancer Res.
, vol.9
, pp. 3329-3337
-
-
Antonescu, C.R.1
-
83
-
-
0032953812
-
Mutations in exon 11 of c-kit occur preferentially in malignant versus benign gastrointestinal stromal tumours and do not occur in leiomyomas or leiomyosarcomas
-
Lasota, J., Jasinski, M., Sarlomo-Rikala, M. & Miettinen, M. Mutations in exon 11 of c-kit occur preferentially in malignant versus benign gastrointestinal stromal tumours and do not occur in leiomyomas or leiomyosarcomas. Am. J. Pathol. 154, 53-60 (1999).
-
(1999)
Am. J. Pathol.
, vol.154
, pp. 53-60
-
-
Lasota, J.1
Jasinski, M.2
Sarlomo-Rikala, M.3
Miettinen, M.4
-
84
-
-
4444379255
-
C-kit gene mutation in human gastrointestinal stromal tumours
-
Hou, Y. Y. et al. C-kit gene mutation in human gastrointestinal stromal tumours. World J. Gastroenterol. 10, 1310-1324 (2004).
-
(2004)
World J. Gastroenterol.
, vol.10
, pp. 1310-1324
-
-
Hou, Y.Y.1
-
85
-
-
0035890740
-
KIT activation is a ubiquitous feature of gastrointestinal stromal tumors
-
Rubin, B. P. et al. KIT activation is a ubiquitous feature of gastrointestinal stromal tumors. Cancer Res. 61, 8118-8121 (2001).
-
(2001)
Cancer Res.
, vol.61
, pp. 8118-8121
-
-
Rubin, B.P.1
|